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    NDC 71863-0109-50 Alkindi 0.5 mg/1 Details

    Alkindi 0.5 mg/1

    Alkindi is a ORAL GRANULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Eton Pharmaceuticals, Inc.. The primary component is HYDROCORTISONE.

    Product Information

    NDC 71863-0109
    Product ID 71863-109_08f49aef-a4f1-da40-e063-6294a90ab218
    Associated GPIs 22100025006810
    GCN Sequence Number 079919
    GCN Sequence Number Description hydrocortisone CAP SPRINK 0.5 MG ORAL
    HIC3 P5A
    HIC3 Description GLUCOCORTICOIDS
    GCN 46547
    HICL Sequence Number 002867
    HICL Sequence Number Description HYDROCORTISONE
    Brand/Generic Brand
    Proprietary Name Alkindi
    Proprietary Name Suffix Sprinkle
    Non-Proprietary Name Hydrocortisone
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form GRANULE
    Route ORAL
    Active Ingredient Strength 0.5
    Active Ingredient Units mg/1
    Substance Name HYDROCORTISONE
    Labeler Name Eton Pharmaceuticals, Inc.
    Pharmaceutical Class Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA213876
    Listing Certified Through 2024-12-31

    Package

    NDC 71863-0109-50 (71863010950)

    NDC Package Code 71863-109-50
    Billing NDC 71863010950
    Package 1 BOTTLE, PLASTIC in 1 CARTON (71863-109-50) / 50 GRANULE in 1 BOTTLE, PLASTIC
    Marketing Start Date 2020-09-29
    NDC Exclude Flag N
    Pricing Information N/A